Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs207482230
rs207482230
TFG
5 0.882 0.080 3 100748182 missense variant C/T snv 4.0E-06 0.800 1.000 6 2012 2017
dbSNP: rs587777789
rs587777789
TFG
3 0.882 0.080 3 100744917 missense variant G/A;T snv 4.0E-06 0.700 0